A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430185



Internal ID209002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:29966914..29966965hg38UCSC Ensembl
chr19:30457821..30457872hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722684
Samples
Known GenesURI1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430185
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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